Canonical Allele Identifier: PA2827975643
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro996Leu
CA16028060
NM_001354899.2:c.2987C>T